Overview of Research Core Unit The Zebrafish Genetics Core is critical to all three Component Projects (CPs). It will provide state-of-the-art resources for working with wildtype and mutant zebrafish lines, and generate the embryos to be analyzed in the three CPs. It will allow the participating investigators to maintain existing wildtype and mutant lines; generate new mutant lines by mutagenesis followed by phenotypic or sequence-based screening; propagate and screen families harboring new mutations; and preserve lines by sperm cryopreservation. It will provide facilities for handling all of the wildtype and mutant crosses for the three CPs, as well as for initial phenotypic analyses. The facility is housed in a newly-renovated 2800 sq ft facility. The Facility Director is a Ph.D. scientist with extensive experience in research and in management of research facilities. She will be assisted by an Assistant Manager who is expert in zebrafish care, a full-time technician responsible for the maintenance of the aquaculture system, and by several helpers who will handle daily animal husbandry including feeding, tank cleaning, etc.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD048886-02
Application #
7610900
Study Section
Pediatrics Subcommittee (CHHD)
Project Start
Project End
Budget Start
2008-03-01
Budget End
2009-02-28
Support Year
2
Fiscal Year
2008
Total Cost
$150,024
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Morrow, Zachary T; Maxwell, Adrienne M; Hoshijima, Kazuyuki et al. (2017) tbx6l and tbx16 are redundantly required for posterior paraxial mesoderm formation during zebrafish embryogenesis. Dev Dyn 246:759-769
Yabe, Taijiro; Hoshijima, Kazuyuki; Yamamoto, Takashi et al. (2016) Quadruple zebrafish mutant reveals different roles of Mesp genes in somite segmentation between mouse and zebrafish. Development 143:2842-52
Ota, Satoshi; Hisano, Yu; Muraki, Michiko et al. (2013) Efficient identification of TALEN-mediated genome modifications using heteroduplex mobility assays. Genes Cells 18:450-8
Wang, Xu; Kopinke, Daniel; Lin, Junji et al. (2012) Wnt signaling regulates postembryonic hypothalamic progenitor differentiation. Dev Cell 23:624-36
Kruse-Bend, Renee; Rosenthal, Jude; Quist, Tyler S et al. (2012) Extraocular ectoderm triggers dorsal retinal fate during optic vesicle evagination in zebrafish. Dev Biol 371:57-65
Xing, Lingyan; Hoshijima, Kazuyuki; Grunwald, David J et al. (2012) Zebrafish foxP2 zinc finger nuclease mutant has normal axon pathfinding. PLoS One 7:e43968
Dahlem, Timothy J; Hoshijima, Kazuyuki; Jurynec, Michael J et al. (2012) Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome. PLoS Genet 8:e1002861
Bisgrove, Brent W; Makova, Svetlana; Yost, H Joseph et al. (2012) RFX2 is essential in the ciliated organ of asymmetry and an RFX2 transgene identifies a population of ciliated cells sufficient for fluid flow. Dev Biol 363:166-78
Demarest, Bradley L; Horsley, Wyatt H; Locke, Erin E et al. (2011) Trans-centromere effects on meiotic recombination in the zebrafish. Genetics 187:333-6
Wythe, Joshua D; Jurynec, Michael J; Urness, Lisa D et al. (2011) Hadp1, a newly identified pleckstrin homology domain protein, is required for cardiac contractility in zebrafish. Dis Model Mech 4:607-21

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